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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06296043
Other study ID # SBU-FUT-01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 10, 2024
Est. completion date August 15, 2024

Study information

Verified date February 2024
Source Saglik Bilimleri Universitesi
Contact Filiz Ünal Toprak, PhD
Phone 05077732090
Email filizore1@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the effect of su-jok application and progressive muscle relaxation exercise in coping with premenstrual syndrome.


Description:

Various medications can be used to relieve PMS symptoms, but there is no treatment to completely eliminate it. For this reason, women may seek traditional and alternative practices to reduce PMS complaints. Alternative methods such as herbal treatment, aromatherapy, acupuncture, nutrition regulation and stress control can be used to relieve PMS symptoms. It has been stated that applying mind-body based therapies to relieve PMS symptoms is safe and cost-effective. Such interventions include progressive muscle relaxation exercise (PCGE), paced breathing, clinical hypnosis, yoga, mindfulness, reflexology, and cognitive behavioral therapies. Su-Jok application, which is an alternative method, can also be used to relieve PMS symptoms. In Su-Jok therapy, the practitioner stimulates points on the hands and feet to activate auto-regulatory mechanisms and bring the body to a healthy state. Due to the negative effects of PMS on daily life, knowing the frequency of occurrence and risk factors is expected to contribute and guide individuals in coping with PMS. While PMS threatens the health of the individual in particular, it generally brings socio-economic burdens to the individual, family and society.


Recruitment information / eligibility

Status Recruiting
Enrollment 135
Est. completion date August 15, 2024
Est. primary completion date July 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Getting over 104 points from the PMS scale, - Having regular menstruation, - Not having any chronic disease, - Not using any method to cope with PMS. Exclusion Criteria: - Having irregular menstruation, - Having musculoskeletal system and respiratory diseases, - Having a diagnosed psychiatric disease, - Having a disease that may cause premenstrual symptoms and receiving medical treatment (thyroid diseases, heart failure, neurological disorders)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Progressive Muscle Relaxation Exercise Group
Exercise Group
Su-Jok Intervention
Hand massage with seeds

Locations

Country Name City State
Turkey Saglik Bilimleri Üniversitesi Ankara

Sponsors (1)

Lead Sponsor Collaborator
Saglik Bilimleri Universitesi

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary PAIN Visual Analog Scale (VAS)- (Min:0 - Max:10) In the 1st, 2nd and 3rd month menstrual periods;
Premenstrual Syndrome Scale
VAS evaluation scale will be applied.
3 months
Primary FATIGUE Visual Analog Scale (VAS)- (Min:0 - Max:10) In the 1st, 2nd and 3rd month menstrual periods;
Premenstrual Syndrome Scale
VAS evaluation scale will be applied.
3 months
Primary SLEEP STATE Visual Analog Scale (VAS)- (Min:0 - Max:10) In the 1st, 2nd and 3rd month menstrual periods;
Premenstrual Syndrome Scale
VAS evaluation scale will be applied.
3 months
Primary NAUSEA VOMITING Visual Analog Scale (VAS)- (Min:0 - Max:10) In the 1st, 2nd and 3rd month menstrual periods;
Premenstrual Syndrome Scale
VAS evaluation scale will be applied.
3 months
Primary Change in Premenstrual Symptoms (People with PMS scale scores over 104 points will be determined). In the 1st, 2nd and 3rd month menstrual periods;
Premenstrual Syndrome Scale
VAS evaluation scale will be applied.
3 months
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